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来自大肠杆菌突变体的RNA合成保真度降低的RNA聚合酶表明,转录过程中存在非互补核苷酸掺入的校正系统。

An RNA polymerase with reduced fidelity of RNA synthesis from an E. coli mutant suggests the existence of a correction system of non-complementary nucleotide incorporation during transcription.

作者信息

Kamzolova S G, Ozoline O N

出版信息

Mol Biol Rep. 1982 Apr 16;8(3):133-5. doi: 10.1007/BF00777239.

Abstract

An RNA polymerase mutant of E. coli B/r-rpoB402, with a pleiotropic effect on stability of the phenotype has recently been obtained (8-11). The present study is concerned with the fidelity of in vitro RNA synthesis carried out by highly purified RNA polymerase from the wild type strain and rpoB402 mutant. The data indicate that mutational alteration of RNA polymerase reduced the accuracy of the enzyme to a value lower than that required for the cell. The results suggest the existence of some correcting system during transcription.

摘要

最近获得了大肠杆菌B/r-rpoB402的一种RNA聚合酶突变体,它对表型稳定性具有多效性影响(8 - 11)。本研究关注的是由野生型菌株和rpoB402突变体的高度纯化RNA聚合酶进行的体外RNA合成的保真度。数据表明,RNA聚合酶的突变改变使该酶的准确性降低到低于细胞所需的值。结果表明转录过程中存在某种校正系统。

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